List of variants in gene KRT1 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_006121.4(KRT1):c.982A>T (p.Thr328Ser)	rs139428176	0.00126
NM_006121.4(KRT1):c.257G>A (p.Arg86His)	rs886049637	0.00003
NM_006121.4(KRT1):c.20C>T (p.Ser7Phe)
NM_006121.4(KRT1):c.481C>T (p.Leu161Phe)

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